WARNING: ALWAYS SPEAK TO YOUR PRESCRIBING PHYSICIAN BEFORE DISCONTINUING ANY MEDICATION
VIOXX and ZYPREXA OUT-OF-COURT SETTLEMENTS
Ellis Law's clients share in $4.85 Billion and $1.2 Billion drug settlements.
Ellis Law is pleased to report that some of our clients have participated in two large defective drug litigation settlements. These include the $4.85 Billion settlement of claims against Merck, in which it was contended that the drug Vioxx caused heart attacks and strokes, along with the $1.2 Billion settlement by Eli Lilly & Co. of claims involving the drug Zyprexa. The initial Zyprexa settlement by Eli Lilly of $690 Million was later increased to $1.2 Billion. The original press release concerning the latter settlement can be read here.
ZOFRAN BIRTH DEFECTS LAWSUIT
Ellis Law is currently accepting clients for a proposed claim involving serious birth defects linked to the anti-nausea drug Zofran taken during pregnancy.
If you took Zofran during your pregnancy and your child was born with a HEART DEFECT, CLEFT LIP, CLEFT PALATE, CLUB FOOT, KIDNEY PROBLEM or has passed away, please submit a FREE INJURY ANSWERLINE (R) inquiry or call us at 1-800-LAW-7777 (1-800-529-7777) or 1-800-3-ABOGADO (1-800-322-6423) immediately!
LOW-TESTOSTERONE or LOW-T THERAPY CASE UNDER INVESTIGATION
Ellis Law is currently accepting clients for a proposed claim involving heart attacks, strokes and/or blood clots alleged to have been caused by low testosterone (Low-T) therapy treatments. If you feel you have been injured by Low-T or any other dangerous or defective drug or other product, please submit a FREE INJURY ANSWERLINE® inquiry or call us at 1-800-LAW-7777 immediately!
OVARIAN CANCER - TALCUM POWDER LAWSUITS
Ellis Law is currently evaluating claims against the manufacturers of talcum powder and other talc products, which some studies have shown to cause ovarian cancer. If you or a loved one has suffered from this terrible type of cancer and previously used talcum powder or other talc products, please submit a FREE INJURY ANSWERLINE® inquiry or call us at 1-800-LAW-7777 (1-800-529-7777, Toll Free Nationwide) or 1-800-3-ABOGADO (1-800-322-6423) immediately!
Claim That Actos Increases Risk Of Bladder Cancer; Lawsuits Underway
$9 BILLION JURY AWARD - ACTOS LAWSUIT RESULT
In the first federal Actos lawsuit to go to trial, in April 2014 a jury in Lafayette, Louisiana (where multidistrict Actos litigation is assigned) has awarded more than $9 Billion in damages on behalf of the plaintiffs against the drug manufacturers. The Louisiana docket lists 2,923 pending Actos cases. This huge victory by the plaintiffs' lawyers who handled that case can only be seen as a "win" for Ellis Law's Actos clients who could benefit from negotiations, which may ensue from this major victory over the drug manufacturers.
Background: The Food and Drug Administration (FDA) reviewed partial findings from a 10-year study by the manufacturer that determined Actos (pioglitazone hydrochloride), the prescription medication used to improve blood sugar level for those with type 2 diabetes, carries with it an increased risk of bladder cancer. The findings of the epidemiological study of 193,099 diabetic patients, which were released this past June, have created enough worry that Actos has already been banned in France and Germany because of its risk. The FDA is now advising doctors to warn patients of the risk when prescribing the medication. Further, the FDA noted in its June 15, 2011, Drug Safety Communication concerning risks of bladder cancer from use of pioglitazone:
"[compared] to never being exposed to pioglitazone, a duration of pioglitazone therapy longer than 12 months was associated with a 40% increase in risk"
Actos belongs to a class of drug known as thiazolidinedione (TZD), which now has two popular drugs associated with severe harmful side effects. Previously, concerns that the other drug in the class, Avandia, may increase the risk of heart attack prompted the FDA to restrict use of the drug. Actos has in some cases been prescribed instead of Avandia because of these concerns. Unfortunately, a recent study published in the American Heart Association journal Circulation found that Actos may also increase the risk of heart disease.
Takeda Pharmaceuticals and Eli Lilly & Co., the manufacturers of Actos, are facing a class-action lawsuit for a failure to warn consumers of the increased risks. In 2009, Eli Lilly & Co. pled guilty to illegally marketing Zyprexa, an antipsychotic drug. Ultimately the company paid out $1.42 Billion to settle the government claims and $1.2 Billion to settle the plaintiffs' claims in the pharmaceutical class action. Ellis Law's Zyprexa clients have shared in the latter settlement.
Takeda Pharmaceuticals has been the sole marketer of Actos since 2006, when Eli Lilly lost its rights to the drug. Actos has been one of the most prescribed drugs in the U.S., with sales in 2010 exceeding $2.6 Billion.
ALWAYS SPEAK TO YOUR PRESCRIBING PHYSICIAN BEFORE DISCONTINUING ANY MEDICATION. If you have symptoms of bladder cancer, such as blood in the urine, pain or burning during urination or a change in bladder habits, speak to a doctor immediately.
Actos is also marketed under the names "Actoplus Met," "Actoplus Met XR" and "Duetact." Anyone who took or is taking Actos or another of these drugs should contact Ellis Law to discuss potential involvement in the class-action suit, which may bring significant compensation for injuries and wrongful death